Journals / GORM:Gynecology Obstetrics & Reproductive Medicine / 2009 / Cilt: 15 - Sayı: 3

Harlequin iktiyozis: Bir olgu sunumu

Harlequin ichtyosis: A case report

Pages
165–167
DOI
—
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In this case report we summarize a patient who delivered a baby with Harlequin ichthyosis.

📌 3 Key Takeaways

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Objective & Hypothesis:Harlequin ichthyosis is a severe and usually fatal congenital keratinization disorder.
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Key Findings & Data:Although it has many characteristic findings on prenatal ultrasound such as a wide gaping mouth, intrauterine growth retardation, short limbs, joint contractures, edema of the hands and feet and cloudy amniotic fluid, most of the time it is diagnosed at birth.
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Conclusion & Impact:In this case report we summarize a patient who delivered a baby with Harlequin ichthyosis.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Harlequin ichthyosis is a severe and usually fatal congenital keratinization disorder. Although it has many characteristic findings on prenatal ultrasound such as a wide gaping mouth, intrauterine growth retardation, short limbs, joint contractures, edema of the hands and feet and cloudy amniotic fluid, most of the time it is diagnosed at birth. In this case report we summarize a patient who delivered a baby with Harlequin ichthyosis.

Özet

Harlequin iktiyozis çok ciddi ve genellikle ölümcül seyreden bir keratinizasyon bozukluğudur. Prenatal ultrasonografide geniş açık ağız, intrauterin gelişme geriliği, kısa kol ve bacaklar, eklem kontraktürleri, el ve ayaklarda ödem ve hiperekojen amniotik sıvı gibi karakteristik bulgular olsa da çoğu olgu doğumda tanı alır. Bu olgu sunumunda harlequin iktiyozis hastası bebek doğuran bir hasta ele alınmıştır.

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Cite This Article

KARASU, Y., İLHAN, T. T., KARADENİZ, R. S., GELİŞEN, O. (2009). Harlequin iktiyozis: Bir olgu sunumu. GORM:Gynecology Obstetrics & Reproductive Medicine, Cilt: 15 - Sayı: 3, 165–167. https://ajindex.com/articles/227036

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References (3)

  1. Choate KA, Williams ML, Elias PM, Khavari PA (1998) Transglutaminase 1 expression in a patient with features of harlequin ichthyosis: case report. J Am Acad Dermatol 38(2 Pt 2):325-329 2. Blanchet-Bardon C, Dumez Y, Labbe´ F, et al. Prenatal diagnosis of harlequin fetus. Lancet 1983
  2. I(8316):132. 3. Akiyama M, Nakagiri-Sugiyama Y, Sakai K, 2005. Mutations in lipid transport ABCA12 in harlequin ichthyosis and functional recovery by corrective gene transfer. J Clin Invest 115: 1777-1785. 4. Akiyama M, Suzumori K, Shimizu H. Prenatal diagnosis of harlequin ichthyosis by the examinations of keratinized hair canals and amniotic fluid cells at 19 weeks’ estimated gestational age. Prenat Diagn 1999
  3. Berg C, Geipel A, Kohl M, et al. 2003. Prenatal sonographic features of Harlequin ichthyosis. Arch Gynecol Obstet 268: 48-51. 6. Bongain A, Benoit B, Ejnes L, Lambert JC, Gillet JY. 2002. Harlequin fetus: three-dimensional sonographic findings and new diagnostic approach. Ultrasound Obstet Gynecol 20: 82-85.